1965
DOI: 10.1016/0032-3950(65)90058-4
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Molecular motion in poly-2,5-difluorostyrene determined by nuclear magnetic resonance

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Cited by 4 publications
(4 citation statements)
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“…The conclusions drawn in this work were confirmed by a subsequent study of the NMR spectra of poly-para-fluorostyrene (I) [322] and poly-2,5-difluorostyrene (II) [35]:…”
Section: Study Of Molecular Motion In Polymers By the Nmr Methodssupporting
confidence: 73%
“…The conclusions drawn in this work were confirmed by a subsequent study of the NMR spectra of poly-para-fluorostyrene (I) [322] and poly-2,5-difluorostyrene (II) [35]:…”
Section: Study Of Molecular Motion In Polymers By the Nmr Methodssupporting
confidence: 73%
“…Usually this process is attributed to the rotational vibration of backbone segments, 2 but some authors have assigned the process to the rotations of side phenyl groups. 13 The peak merges into the R peak at high frequencies. 2 Mechanical-relaxation 1 and NMR experiments 14 revealed additional γ and δ processes associated with oscillatory motions of the side phenyl groups.…”
Section: Introductionmentioning
confidence: 96%
“…Relaxational processes in amorphous PS in the vicinity of T g have been studied experimentally by dynamic mechanical, 1-3 quasielastic neutron scattering, 4,5 dielectric, [6][7][8][9][10][11][12] and NMR techniques. [13][14][15][16] It is an established fact that above the PS glass-transition temperature (T g ) 373 K), the R-relaxation is the primary relaxation process of collective segmental motion, 32 and the temperature dependence of the characteristic relaxation times is well described by WLF equation. 33 Immediately below (when decreasing temperature) the primary relaxation, there is another, so-called process, which appears in both dynamic mechanical and dielectric experiments.…”
Section: Introductionmentioning
confidence: 99%
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